Use my Search Websuite to scan PubMed, PMCentral, Journal Hosts and Journal Archives, FullText. Kick-your-searchterm to multiple Engines kick-your-query now !>

A dictionary by aggregated review articles of nephrology, medicine and the life sciences Your one-stop-run pathway from word to the immediate pdf of peer-reviewed on-topic knowledge.

10.1161/ATVBAHA.116.308039 http://scihub22266oqcxt.onion/10.1161/ATVBAHA.116.308039 C5001918!5001918!27444200     free     free     free Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 243.2 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 243.2 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 243.2 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Arterioscler+Thromb+Vasc+Biol 2016 ; 36 (9): 1910-8 Nephropedia Template TP {{tp|p=27444200|t=2016. Significant Differences in Antigen-induced Transendothelial Migration of Human CD8 and CD4 T Effector Memory Cells |pdf=|usr=}}{{27444200}} gab.com Text Significant Differences in Antigen-induced Transendothelial Migration of Human CD8 and CD4 T Effector Memory Cells JO: Arterioscler Thromb Vasc Biol http://www.kidney.de/pget.php?&tw=1&pmid=27444200 #FOAvip Objective: Circulating human T effector memory cell (TEM) recognition of non-self MHC molecules on allograft endothelial cells (EC) can initiate graft rejection despite elimination of professional antigen presenting cells necessary for naïve T cell activation. Our prior studies of CD4 TEM have established that engagement of the T cell receptor (TCR) not only activates T cells but also triggers transendothelial migration (TEM) by a process that is distinct from that induced by activating chemokine receptors (CR) on T cells, being slower, requiring microtubule organizing center (MTOC)-directed cytolytic granule polarization to and release from the leading edge of the T cell, and requiring engagement of proteins of the EC lateral border recycling compartment (LBRC). While CD4 TEM may contribute to acute allograft rejection, the primary effectors are alloreactive CD8 TEM. Whether and how TCR engagement affects TEM of human CD8 TEM is unknown. Approach and Results: We modeled TEM of CD8 TEM across cultured human microvascular EC engineered to present superantigen under conditions of venular shear stress in vitro in a flow chamber. Here we report that TCR engagement can also induce TEM of this population that similarly differs from CR-driven TEM with regard to kinetics, morphological manifestations, and MTOC dynamics as with CD4 TEM. However, CD8 TEM do not require either cytolytic granule release or interactions with proteins of the LBRC. Conclusions: These results imply that therapeutic strategies designed to inhibit TCR-driven recruitment based on targeting granule release or components of the LBRC will not affect CD8 TEM and are unlikely to block acute rejection in the clinic. Twit Text FOAVip Significant Differences in Antigen-induced Transendothelial Migration of Human CD8 and CD4 T Effector Memory Cells ????Arterioscler Thromb Vasc Biol http://www.kidney.de/pget.php?&tw=1&pmid=27444200 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27444200 #FOAvip English Wikipedia <ref>{{Cite pmid|27444200}}</ref> Significant Differences in Antigen-induced Transendothelial Migration of Human CD8 and CD4 T Effector Memory Cells #MMPMID27444200 Manes TD; Pober JS Arterioscler Thromb Vasc Biol 2016[Sep]; 36 (9): 1910-8 PMID27444200show ga Objective: Circulating human T effector memory cell (TEM) recognition of non-self MHC molecules on allograft endothelial cells (EC) can initiate graft rejection despite elimination of professional antigen presenting cells necessary for naïve T cell activation. Our prior studies of CD4 TEM have established that engagement of the T cell receptor (TCR) not only activates T cells but also triggers transendothelial migration (TEM) by a process that is distinct from that induced by activating chemokine receptors (CR) on T cells, being slower, requiring microtubule organizing center (MTOC)-directed cytolytic granule polarization to and release from the leading edge of the T cell, and requiring engagement of proteins of the EC lateral border recycling compartment (LBRC). While CD4 TEM may contribute to acute allograft rejection, the primary effectors are alloreactive CD8 TEM. Whether and how TCR engagement affects TEM of human CD8 TEM is unknown. Approach and Results: We modeled TEM of CD8 TEM across cultured human microvascular EC engineered to present superantigen under conditions of venular shear stress in vitro in a flow chamber. Here we report that TCR engagement can also induce TEM of this population that similarly differs from CR-driven TEM with regard to kinetics, morphological manifestations, and MTOC dynamics as with CD4 TEM. However, CD8 TEM do not require either cytolytic granule release or interactions with proteins of the LBRC. Conclusions: These results imply that therapeutic strategies designed to inhibit TCR-driven recruitment based on targeting granule release or components of the LBRC will not affect CD8 TEM and are unlikely to block acute rejection in the clinic. äSignificant Differences in Antigen-induced Transendothelial Migration (epmc).pdf DeepDyve Pubget Overpricing